F14V (p.Phe14Val) variant of SLC37A4 (O43826)
F14V (p.Phe14Val) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
F14V (p.Phe14Val) variant details
- p.Phe14Val
- TOPMed rs1478775690
- gnomAD rs1478775690
- Missense
- Variant Prioritization Score for Impact Estimate 0.663
- CADD 28.60
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available